Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs2004640 0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs2276109 0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 18
rs35705950 0.763 0.240 11 1219991 splice region variant G/A;T snv 14
rs10168266 0.776 0.400 2 191071078 intron variant C/T snv 0.19 8
rs1059702 0.807 0.280 X 154018741 missense variant A/G snv 0.72 7